| NDC Code | 23731-6051-2 |
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| Package Description | 25 VIAL, SINGLE-USE in 1 CASE (23731-6051-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3) |
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| Product NDC | 23731-6051 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Anticoagulant Citrate Dextrose A |
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| Non-Proprietary Name | Anhydrous Citric Acid, Dextrose Monohydrate, And Trisodium Citrate Dihydrate |
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| Dosage Form | SOLUTION |
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| Usage | EXTRACORPOREAL |
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| Start Marketing Date | 20030826 |
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| Marketing Category Name | NDA |
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| Application Number | BN020037 |
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| Manufacturer | Citra Labs LLC |
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| Substance Name | ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
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| Strength | .073; .245; .22 |
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| Strength Unit | g/10mL; g/10mL; g/10mL |
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| Pharmacy Classes | Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE] |
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